Human Genome Epidemiology Literature Finder
|
Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and LAMA1[original query] |
|---|
| The association of a single nucleotide polymorphism in the promoter region of the LAMA1 gene with susceptibility to Chinese high myopia. Molecular vision 2011 17 . Zhao YY, Zhang FJ, Zhu SQ, Duan H, Li Y, Zhou ZJ, Ma WX, Li Wang N |
Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.
Translational psychiatry 2012 2 e129. Adkins D E, Clark S L, Åberg K, Hettema J M, Bukszár J, McClay J L, Souza R P, van den Oord E J C |
| Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.
PLoS genetics 2012 May 8 (5): e1002741. Perry John R B, Voight Benjamin F, Yengo Loïc, Amin Najaf, Dupuis Josée, Ganser Martha, Grallert Harald, Navarro Pau, Li Man, Qi Lu, Steinthorsdottir Valgerdur, Scott Robert A, Almgren Peter, Arking Dan E, Aulchenko Yurii, Balkau Beverley, Benediktsson Rafn, Bergman Richard N, Boerwinkle Eric, Bonnycastle Lori, Burtt Noël P, Campbell Harry, Charpentier Guillaume, Collins Francis S, Gieger Christian, Green Todd, Hadjadj Samy, Hattersley Andrew T, Herder Christian, Hofman Albert, Johnson Andrew D, Kottgen Anna, Kraft Peter, Labrune Yann, Langenberg Claudia, Manning Alisa K, Mohlke Karen L, Morris Andrew P, Oostra Ben, Pankow James, Petersen Ann-Kristin, Pramstaller Peter P, Prokopenko Inga, Rathmann Wolfgang, Rayner William, Roden Michael, Rudan Igor, Rybin Denis, Scott Laura J, Sigurdsson Gunnar, Sladek Rob, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Tuomilehto Jaakko, Uitterlinden Andre G, Vivequin Sidonie, Weedon Michael N, Wright Alan F, , , , Hu Frank B, Illig Thomas, Kao Linda, Meigs James B, Wilson James F, Stefansson Kari, van Duijn Cornelia, Altschuler David, Morris Andrew D, Boehnke Michael, McCarthy Mark I, Froguel Philippe, Palmer Colin N A, Wareham Nicholas J, Groop Leif, Frayling Timothy M, Cauchi Stépha |
| Laminin-1 (LM-111) in preeclampsia and systemic lupus erythematosus. Autoimmunity 2012 Oct . Páez MC, Matsuura E, Díaz LA, Shoenfeld Y, Serrano NC, Anaya JM |
| Replication Study in a Japanese Population to Evaluate the Association between 10 SNP Loci, Identified in European Genome-Wide Association Studies, and Type 2 Diabetes. PloS one 2015 10 (5): e0126363. Matsuba Ren, Sakai Kensuke, Imamura Minako, Tanaka Yasushi, Iwata Minoru, Hirose Hiroshi, Kaku Kohei, Maegawa Hiroshi, Watada Hirotaka, Tobe Kazuyuki, Kashiwagi Atsunori, Kawamori Ryuzo, Maeda Shi |
| Examination of candidate exonic variants for association to Alzheimer disease in the Amish. PloS one 2015 10 (2): e0118043. D'Aoust Laura N, Cummings Anna C, Laux Renee, Fuzzell Denise, Caywood Laura, Reinhart-Mercer Lori, Scott William K, Pericak-Vance Margaret A, Haines Jonathan |
| Targeted next generation sequencing in 112 Chinese patients with intellectual disability/developmental delay: novel mutations and candidate gene. BMC medical genetics 2019 5 20 (1): 80. Yan Huifang, Shi Zhen, Wu Ye, Xiao Jiangxi, Gu Qiang, Yang Yanling, Li Ming, Gao Kai, Chen Yinyin, Yang Xiaoping, Ji Haoran, Cao Binbin, Duan Ruoyu, Jiang Yuwu, Wang Jingm |
| Whole exome sequencing identifies the novel putative gene variants related with type 2 diabetes in Mizo population, northeast India. Gene 2020 10 769 145229. Lalrohlui Freda, Zohmingthanga John, Hruaii Vanlal, Vanlallawma Andrew, Senthil Kumar Nachimut |
| Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy. Frontiers in molecular neuroscience 2022 6 15 825390. Luo Sheng, Liu Zhi-Gang, Wang Juan, Luo Jun-Xia, Ye Xing-Guang, Li Xin, Zhai Qiong-Xiang, Liu Xiao-Rong, Wang Jie, Gao Liang-Di, Liu Fu-Li, Ye Zi-Long, Li Huan, Gao Zai-Fen, Guo Qing-Hui, Li Bing-Mei, Yi Yong-Hong, Liao Wei-Pi |
- Page last reviewed:Feb 1, 2024
- Content source: